Laurie Lea Williamson v. State

CourtCourt of Appeals of Texas
DecidedMay 6, 2010
Docket01-08-00366-CR
StatusPublished

This text of Laurie Lea Williamson v. State (Laurie Lea Williamson v. State) is published on Counsel Stack Legal Research, covering Court of Appeals of Texas primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Laurie Lea Williamson v. State, (Tex. Ct. App. 2010).

Opinion

Opinion to issue May 6, 2010




In The

Court of Appeals

For The

First District of Texas





NO. 01-08-00365-CR

NO. 01-08-00366-CR





LAURIE LEA WILLIAMSON, Appellant,


V.


THE STATE OF TEXAS, Appellee





On Appeal from the 184th District Court

Harris County, Texas

Trial Court Cause Nos. 1110103 & 1110104





O P I N I O N

          These two appeals involve allegations that the complainant, C.W., was the victim of medical child abuse, sometimes referred to as Munchausen Syndrome by Proxy, perpetrated by his mother, appellant, Laurie Lea Williamson. The bases for the criminal charges against appellant are two surgical procedures performed on C.W. in 2001, when he was five and six years old. The State offered evidence at trial to show that the surgeries were not medically necessary and that appellant knowingly and intentionally caused the unnecessary procedures to be performed by fabricating, exaggerating, and inducing the symptoms leading to the surgeries.

          Following a joint trial on two separate indictments, a jury found appellant guilty of two first-degree felony offenses of injury to a child, as alleged in each indictment. See Tex. Penal Code Ann. § 22.04(a)(1), (c)(1), (e) (Vernon Supp. 2009). Because each indictment alleged that appellant had caused C.W. serious bodily injury by “cutting him with a deadly weapon, namely, a scalpel,” the trial court included in each judgment an affirmative deadly-weapon finding. The jury assessed punishment at 15 years’ imprisonment for each offense, with the sentences to run concurrently. Appealing each judgment of conviction, appellant raises seven identical issues in each appeal.

          We affirm the judgment in each appellate cause.

Background

          Appellant and her husband had two sons: the complainant, C.W., born on March 16, 1995, and D.W., born on May 21, 1997. They also had one daughter, L.W., born on September 1,1999. After L.W. was born, appellant divorced the children’s father and became the children’s primary care giver.

          By the time he was five years old, C.W. already had been diagnosed with a number of medical problems, including Crohn’s disease, which is an intestinal disorder, Tourette’s Syndrome, attention deficit hyperactivity disorder, and obsessive compulsive disorder. C.W. took a number of medications for these afflictions.

          Appellant also reported to C.W.’s doctors that C.W. suffered from “staring spells,” in which C.W. would stare, “zone out,” and be non-responsive. After these spells, appellant claimed that C.W. would often fall asleep and lose bladder control. These episodes reported by appellant were diagnosed as “partial complex seizures,” a form of epilepsy.

          For his seizures, C.W. was referred to Dr. Balbir Singh, a neurologist, who specializes in pediatric epilepsy. During C.W.’s first visit, Dr. Singh noticed that C.W. appeared to be “doped up” or over-medicated. C.W. was drowsy and unsteady on his feet. Dr. Singh ordered a blood test, which revealed that C.W. had levels of Dilantin, an anti-seizure medication, at twice the recommended level.

          Dr. Singh tried to control C.W.’s seizures with medications. Appellant continued to report to the doctor that C.W. experienced seizures. Several medical tests were performed on C.W., including electroencephalography (EEG) tests. An EEG is an electrical test of the brain, which can aid in determining whether a person has seizure activity.

          The EEG tests performed on C.W. were not definitive. At least one of the tests indicated abnormal “generalized epileptic form activity,” which showed a correlation with seizure activity. Other EEG tests performed on C.W. indicated no abnormal activity. Dr. Singh had a video EEG performed on C.W. over a 23-hour period. During that period, appellant reported that C.W. had three or four seizures, but none were recorded on the EEG.

          Despite the fact that Dr. Singh had C.W. on the maximum dosages for ani-seizure medications, appellant reported that C.W. continued to have up to 11 seizures a day. Based primarily on appellant’s report of the continued seizure activity, Dr. Singh referred C.W. to a surgeon for the implantation of a vagal nerve stimulator, a device that can decrease seizure activity when medications have failed. At trial, Dr. Singh testified that the vagal nerve is the nerve that runs from the brain to the stomach. With regard to the procedure, the doctor explained that the vagal nerve stimulator is a device that “can be inserted just under the skin . . . and then a wire goes from the device to the nerve” and “then winds around the nerve.” He continued, “[T]he device stimulates the nerve every one minute or every 10 minutes. We can program the device from the outside.” Dr. Singh further explained that “we can change the settings of the [vagal nerve stimulator] device to give the shocks at different times and different strengths.”

          A surgeon, Dr. James Baumgartner, implanted the vagal nerve stimulator on January 5, 2001. Dr. Singh set the vagal nerve stimulator at different strengths but the device did not stop the seizures, according to appellant. The device was deactivated six weeks after it was implanted and was never reactivated. Appellant continued to report that C.W. suffered from seizures.

          C.W. was hospitalized in February 2001 with a “failure to thrive” diagnosis, which meant that C.W. was not growing properly. A pediatric surgeon, Dr. Paul Minifee, surgically placed a central line into C.W.’s subclavian vein to provide C.W. nutrition. While he was hospitalized, C.W. was seen by many specialists from several disciplines, including neurology, endocrinology, hematology, oncology, and genetics. A concern was raised by the neurology team that perhaps C.W. was a victim of Munchausen Syndrome by Proxy by appellant. The doctors had a child protection meeting, and it was decided that they did not have enough evidence to make a Munchausen Syndrome by Proxy diagnosis.

          Prior to C.W.’s discharge from the hospital, Dr. Minifee placed a nasal gastric feeding tube through C.W.’s nose, down his throat, and into his stomach. The purpose of the tube was for C.W. to be fed liquid formula.

          Around this time period, others also had concerns for C.W.’s welfare. When C.W. was in preschool, he was a happy, spunky, smart preschooler. C.W.

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